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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
Amyotrophic Lateral Sclerosis 1
USH2A c.8559-2A>G
Cystic Fibrosis
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Gene editing
Ercc2
tm1Jmch
Alias:
XPD
R683W
XPD
+XP
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Basic Information
Phenotypes
References Literature
A targeting vector was designed to insert the R683W substitution into exon 22. RT-PCR confirmed expression of the mutant transcript from ES cells. The neo cassette was not removed from this allele. (J:116054)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
3693615
129
Targeted
Insertion, Nucleotide substitutions
--
1
12
1
Phenotypes
Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes
References Literature
Title
PMID
Journal
Year
IF
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